SAN DIEGO, Aug. 18, 2023 /PRNewswire/ -- Arthrosi Therapeutics, Inc., a clinical-stage biotechnology company, has announced they have received written response from the U.S. Food and Drug Administration (FDA) related to their End-of-Phase 2 briefing package for AR882, its lead drug candidate for gout treatment. AR882 is a highly potent, selective, and once daily dosing next-gen URAT1 inhibitor. The feedback from the FDA supports Arthrosi progressing with its planned Phase 3 clinical program.  

"We were pleased with the response from the FDA on the end-of-phase 2 strategy for nonclinical and clinical development of AR882," noted Litain Yeh, PhD, CEO of Arthrosi. "We look forward to our upcoming Phase 3 clinical trial, with the intent of accumulating robust data that could pave the way to enriching the treatment landscape for gout patients. There is a clear and pressing need for innovative therapies, like AR882, for patients struggling with gout."

The company remains committed to progressing its research, with the overarching goal of improving gout treatment options and patient outcomes.